DisGeNET - a database of gene-disease associations

Source: ORPHANET

Disease: Leber Congenital Amaurosis ×

Gene: GUCY2D ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	3000
Gene Symbol:	GUCY2D

GUCY2D

CUI:	C0339527
Disease:	Leber Congenital Amaurosis

Leber Congenital Amaurosis

0.500

GermlineCausalMutation

ORPHANET

Review and update on the molecular basis of Leber congenital amaurosis.

2015